Teams at Rhythm Pharmaceuticals

Provide legal support for global clinical operations including drafting, reviewing, and negotiating clinical trial contracts (CROs, sites, vendors), lead CLM processes and playbooks, advise business leaders on risk-based strategies, manage outside counsel, and contribute to cross-functional life sciences legal matters.

Lead design, execution, and interpretation of mechanistic and translational in vitro and in vivo studies via CROs and collaborators to inform discovery and early-stage development. Identify and prioritize exploratory biology initiatives, develop hypotheses and assays, integrate multidisciplinary data, guide program strategy, and communicate findings to senior leadership while managing external partners and cross-functional teams.

Lead GCP/GLP/GVP quality oversight for clinical studies, manage QMS and vendor audit programs, develop SOPs and training, support regulatory inspections, review clinical and safety documents, identify and mitigate compliance risks, and partner cross-functionally to ensure GCP compliance and quality across programs.